Canonical Allele Identifier: PA2825492903
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg367Cys
CA014305
NM_001099405.2:c.1099C>T
CA645519439
NM_001099405.2:c.1098_1099delinsTT